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Details

Stereochemistry ABSOLUTE
Molecular Formula C22H28FO8P.2Na
Molecular Weight 516.4046
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PARAMETHASONE DISODIUM PHOSPHATE

SMILES

[Na+].[Na+].C[C@@H]1C[C@H]2[C@@H]3C[C@H](F)C4=CC(=O)C=C[C@]4(C)[C@H]3[C@@H](O)C[C@]2(C)[C@@]1(O)C(=O)COP([O-])([O-])=O

InChI

InChIKey=MHQJKNHAJIVSPW-ZDKQYMEBSA-L
InChI=1S/C22H30FO8P.2Na/c1-11-6-14-13-8-16(23)15-7-12(24)4-5-20(15,2)19(13)17(25)9-21(14,3)22(11,27)18(26)10-31-32(28,29)30;;/h4-5,7,11,13-14,16-17,19,25,27H,6,8-10H2,1-3H3,(H2,28,29,30);;/q;2*+1/p-2/t11-,13+,14+,16+,17+,19-,20+,21+,22+;;/m1../s1

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.98976928
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C22H28FO8P
Molecular Weight 470.4251
Charge -2
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 9 / 9
E/Z Centers 0
Optical Activity UNSPECIFIED

Paramethasone is a glucocorticoid. It exerts anti-inflammatory and immunosuppressant actions. Paramethasone stimulates the synthesis of enzymes needed to decrease anti-inflammatory response. It suppresses the immune system by reducing activity and volume of the lymphatic system, thus producing lymphocytopenia decreasing passage of immune complexes and possibly by depressing reactivity of tissue to antigen-antibody interactions.

Approval Year

PubMed

PubMed

TitleDatePubMed
Adalimumab for the treatment of fistulas in patients with Crohn's disease.
2009-07
Epidural dextran-40 and paramethasone injection for treatment of spontaneous intracranial hypotension.
2006-06
[Hiccups crisis following paramethasone intraarticular injection].
2005-06-25
Surgical decompression versus local steroid injection in carpal tunnel syndrome: a one-year, prospective, randomized, open, controlled clinical trial.
2005-02
Tachon's syndrome (suracute back and/or thoracic pain following local injections of corticosteroids). A report of 318 French cases.
2005-01
[Chronic adhesive arachnoiditis following epidural paramethasone].
1997-12
Two cases of specific adverse reactions to systemic corticosteroids.
1996-09-01
Pseudo-allergic reactions to corticosteroids: diagnosis and alternatives.
1995-05-01
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:32:37 GMT 2025
Edited
by admin
on Mon Mar 31 21:32:37 GMT 2025
Record UNII
41I31208JK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PREGNA-1,4-DIENE-3,20-DIONE, 6-FLUORO-11,17-DIHYDROXY-16-METHYL-21-(PHOSPHONOOXY)-, DISODIUM SALT, (6.ALPHA.,11.BETA.,16.ALPHA.)-
Preferred Name English
PARAMETHASONE DISODIUM PHOSPHATE
WHO-DD  
Common Name English
Paramethasone disodium phosphate [WHO-DD]
Common Name English
Code System Code Type Description
EVMPD
SUB03646MIG
Created by admin on Mon Mar 31 21:32:37 GMT 2025 , Edited by admin on Mon Mar 31 21:32:37 GMT 2025
PRIMARY
ECHA (EC/EINECS)
218-410-5
Created by admin on Mon Mar 31 21:32:37 GMT 2025 , Edited by admin on Mon Mar 31 21:32:37 GMT 2025
PRIMARY
EPA CompTox
DTXSID10944042
Created by admin on Mon Mar 31 21:32:37 GMT 2025 , Edited by admin on Mon Mar 31 21:32:37 GMT 2025
PRIMARY
CAS
2145-14-4
Created by admin on Mon Mar 31 21:32:37 GMT 2025 , Edited by admin on Mon Mar 31 21:32:37 GMT 2025
PRIMARY
SMS_ID
100000085518
Created by admin on Mon Mar 31 21:32:37 GMT 2025 , Edited by admin on Mon Mar 31 21:32:37 GMT 2025
PRIMARY
PUBCHEM
16509
Created by admin on Mon Mar 31 21:32:37 GMT 2025 , Edited by admin on Mon Mar 31 21:32:37 GMT 2025
PRIMARY
FDA UNII
41I31208JK
Created by admin on Mon Mar 31 21:32:37 GMT 2025 , Edited by admin on Mon Mar 31 21:32:37 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY